A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15248314



Internal ID5536501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:51022337..51086008hg38UCSC Ensembl
chr15:51314534..51378205hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3863672
hg1963672
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636460
Supporting Variants
SamplesNA19000
Known GenesTNFAIP8L3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15248314
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer